Saeki Chisato, Oikawa Tsunekazu, Ueda Kaoru, Nakano Masanori, Torisu Yuichi, Saruta Masayuki, Tsubota Akihito
Division of Gastroenterology and Hepatology, Department of Internal Medicine, The Jikei University School of Medicine, 3-25-8 Nishi-shimbashi, Minato-ku, Tokyo 105-8461, Japan.
Division of Gastroenterology, Department of Internal Medicine, Fuji City General Hospital, 50 Takashima-cho, Fuji-shi, Shizuoka 417-8567, Japan.
Diagnostics (Basel). 2022 Aug 12;12(8):1957. doi: 10.3390/diagnostics12081957.
Insulin-like growth factor 1 (IGF-1) plays an important role in bone growth and maintenance, and its decreased levels are associated with bone disorders. This study aimed to evaluate the association of serum IGF-1 levels with osteoporosis, prevalent fractures and fracture risk based on the Fracture Risk Assessment Tool (FRAX) in patients with primary biliary cholangitis (PBC). This study included 127 consecutive patients with PBC. Based on the baseline serum IGF-1 levels, the participants were classified into the low (L)-, intermediate (I)- and high (H)-IGF-1 groups. According to the FRAX score, high fracture risk was defined as a 10-year major osteoporotic fracture probability (FRAX-MOF) ≥ 20% or a 10-year hip fracture probability (FRAX-HF) ≥ 3%. The serum IGF-1 levels were positively correlated with bone mineral density, and were negatively correlated with the FRAX-MOF/FRAX-HF. The L-IGF-1 group had the highest prevalence of osteoporosis (58.1%), prevalent fracture (48.4%) and high fracture risk (71.0%). Meanwhile, the H-IGF-1 group had the lowest prevalence of osteoporosis (9.7%), prevalent fracture (12.9%) and high fracture risk (9.7%). The prevalence of these events increased stepwise with decreasing serum IGF-1 levels. The cutoff values of IGF-1 for predicting osteoporosis, prevalent fracture and high fracture risk were 61.5 ng/mL (sensitivity/specificity, 0.545/0.894), 69.5 ng/mL (0.633/0.784) and 61.5 ng/mL (0.512/0.929), respectively. Serum IGF-1 levels were associated with bone disorders and the FRAX-derived fracture risk, and may be a useful indicator for initiating therapeutic intervention to prevent the incidence of fracture in patients with PBC.
胰岛素样生长因子1(IGF-1)在骨骼生长和维持中起重要作用,其水平降低与骨骼疾病相关。本研究旨在基于骨折风险评估工具(FRAX)评估原发性胆汁性胆管炎(PBC)患者血清IGF-1水平与骨质疏松症、既往骨折及骨折风险之间的关联。本研究纳入了127例连续的PBC患者。根据基线血清IGF-1水平,参与者被分为低(L)-、中(I)-和高(H)-IGF-1组。根据FRAX评分,高骨折风险定义为10年主要骨质疏松性骨折概率(FRAX-MOF)≥20%或10年髋部骨折概率(FRAX-HF)≥3%。血清IGF-1水平与骨密度呈正相关,与FRAX-MOF/FRAX-HF呈负相关。L-IGF-1组骨质疏松症患病率最高(58.1%)、既往骨折患病率最高(48.4%)和高骨折风险患病率最高(71.0%)。同时,H-IGF-1组骨质疏松症患病率最低(9.7%)、既往骨折患病率最低(12.9%)和高骨折风险患病率最低(9.7%)。这些事件的患病率随着血清IGF-1水平的降低而逐步增加。预测骨质疏松症、既往骨折和高骨折风险的IGF-1截断值分别为61.5 ng/mL(敏感性/特异性,0.545/0.894)、69.5 ng/mL(0.633/0.784)和61.5 ng/mL(0.512/0.929)。血清IGF-1水平与骨骼疾病及FRAX衍生的骨折风险相关,可能是启动治疗干预以预防PBC患者骨折发生率的有用指标。